Dry root rot of chillies, caused by Sclerotium rolfsii, is a major disease in chilli-growing areas of Andhra Pradesh, and causes severe losses. The pathogen survives as sclerotia in soil for a long duration which served as a source of primary inoculum (Shoeraj Singh et al, 2007). Due to prolonged, saprophytic survivability of the pathogen, chemical management is not very effective and is, therefore, uneconomical. Plant derivatives endowed with pesticidal properties are being evolved worldwide as alternatives or supplements to existing chemical pesticides for several reasons, viz., spiralling costs, environmental hazards and development of resistance by pathogens and insects (Mishra, 2005). Plant extracts are known to possess antimicrobial properties and several research workers have studied antifungal activity of various plant extracts (Seshakiran et al, 2006; Sheoraj Singh et al, 2007; Deepak Kumar et al, 2008). These reports prompted the present investigation on in vitro screening of plant extracts, viz., neem (Azadirachta indica), bottlebrush (Callistemon lanceolatus De), periwinkle (Vinca rosea), ashoka (Polyalthia longifolia), curry leaf (Murraya koenigii), prosopis (Prosopis julifera), onion bulb (Allium cepa) and ginger stem (Zingiber officinalis) to assess their inhibitory effect on pathogen mycelial growth, sclerotial production and sclerotial germination. Plant extracts: Leaves of neem, Callistemon, Vinca, ashoka, curry plant and Prosopis plants and onion bulb and ginger stem were washed with sterilized distilled water and Short communication Effect of various plant extracts on dry root rot of chillies caused by Sclerotium rolfsii G. Bindu Madhavi, S.L. Bhattiprolu and V. Bali Reddy Regional Agricultural Research Station, Lam Guntur - 522 034, India E-mail : gopireddy_bindu@yahoo.co.in ABSTRACT Eight different plant extracts were evaluated in vitro against Sclerotium rolfsii causing dry root rot in chillies. Among these, leaf extract of neem (Azadirachta indica) caused maximum inhibition of mycelial growth (80.74%), followed by periwinkle Vinca rosea (78.8%) and bottlebrush (Callistemon, 74.8%) respectively. Sclerotial production was inhibited to an extent of 11% and the inhibition caused was maximum with neem extract, followed by Polyalthia longifolia and V. rosea extracts. Though sclerotial germination was inhibited by 30% to 95% in various treatments, the most effective treatment was that of neem leaf extract (95%), followed by ginger extract (92%). Key words: Sclerotium rolfsii, plant extracts, mycelial growth, sclerotial production air-dried. A hundred grams of freshly-chopped leaves, bulb and stem were taken and boiled at 80oC for 10 min. in water. The material was homogenized for five min., filtered through muslin cloth and the filtrate was centrifuged at 5000rpm for 15 min. The clear supernatant was collected and used as 100% standard extract. For evaluation of antifungal activity of these extracts, 10% concentration was made by adding 10ml of standard, basic stock of plant extract to 90ml Potato Dextrose Agar (PDA) in Petri plates, replicated thrice for each treatment. PDA without the plant extract served as the Check. Each plate was inoculated with a sclerotium taken from 15-day old culture of S. rolfsii. Inoculated plates were incubated at 25+1oC and data on (i) mycelial growth and (ii) sclerotial formation were recorded. Sclerotial germination was recorded by collecting sclerotia from 15- day old cultures of the pathogen grown on PDA medium. The sclerotia were at first surface-sterilized with sodium hypochlorite solution (0.35% available chlorine) and then washed in sterile distilled water and placed in sterilized Petri plates under dry conditions. Three sclerotia were suspended in aqueous extracts obtained from the above plant material in the cavities of cavity slides placed over a V- shaped glass rod in a humidity chamber made in sterile Petri plates. The plates were incubated at 28+1oC for 72 hours. A check was also maintained with sterilized distilled water in place of aqueous extract. Each treatment was replicated thrice, germination of sclerotia was recorded and per cent inhibition calculated. J. Hortl. Sci. Vol. 6(2):156-158, 2011 Prinect Color Editor Page is color controlled with Prinect Color Editor 4.0.70 Copyright 2008 Heidelberger Druckmaschinen AG http://www.heidelberg.com You can view actual document colors and color spaces, with the free Color Editor (Viewer), a Plug-In from the Prinect PDF Toolbox. Please request a PDF Toolbox CD from your local Heidelberg office in order to install it on your computer. 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Mycelial growth inhibition ranged from 35.18 to 80.74% (Table1). Significantly, highest inhibition was recorded in the extract obtained from neem leaves (80.1%). Next in order were extracts obtained from Periwinkle (78.8%), Callistemon (74.8%), Ashoka (67.03%), Prosopis spp (52.59%) and Ginger (48.22%). Curry leaf extract was least inhibitory, as was the extract of onion bulbs. The plant extracts did not affect sclerotial formation, although these delayed sclerotial formation by 20 days. Maximum reduction (Table1) in sclerotial formation (11%) was recorded in plates amended with neem leaf extract, followed by Ashoka (9.83%) and Vinca (6.67%). Aqueous extract of neem leaves inhibited sclerotial germination in S. rolfsii by 95%. This was followed by ginger (92%) and Vinca (88%), whereas foliar extracts of ashoka and prosopis recorded 70% and 50% inhibition, respectively. Inhibition of sclerotial germination was low with extracts of onion bulb (Allium cepa, 45%) and bottlebrush (Callistemon lanceolatus De, 40%) whereas, it was least with extract of curry leaf (30%). These results are in agreement with findings of Shoeraj Singh et al (2007) who reported that foliar extract of neem followed by that of ashoka, caused maximum inhibition of mycelial growth, sclerotial production and viability of S. rolfsii causing collar rot of lentil. Seshakiran et al (2006) found mycelial growth and sclerotial formation to be inhibited by extracts of prosopis, neem and onion bulb, as also recorded in the present investigation. Sonali and Gupta (2004) reported that acqueous extracts of mustard cake and neem cake, neem oil reduced in vitro germination of sclerotia of S. rolfsii causing seedling blight of apple. Fungitoxic properties of Prosopsis julifera against various species of Fusarium, Dreschlera and Alternaria were reported by Raghavendra et al (2002) and Ganesan (1993), whereas Datar et al (1999) reported fungicidal properties of leaf extracts of ashoka (Polyalthia longifolia) against Macrophomina phaseolina. Sharma and Gupta (1995) observed decrease in root rot incidence in apple using neem cake as an organic amendment. Similar report came form Karthikeyan and Karunanidhi (1996) with work on several soil-borne pathogens. Singh and Dwivedi (1989) found that Azadirachta indica, Emblica officinalis, turmeric and ginger extracts reduced hyphal dry-weight and sclerotial production in vitro in S. rolfsii. Leaf, flower, stem and root extracts of Vinca rosea were found to be inhibitory to S. rolfsii, Fusarium oxysporum and Aspergillus niger (Narain and Satapathy, 1977). Findings in the present study are in conformity with those in the above-stated reports and these can be further exploited for formulating integrated disease management (IDM) schedule for dry root rot of chillies. REFERENCES Datar, V.V, 1999. Bioefficacy of plant extracts against Macrophomina phaseolina (Tassi) Gold, the incitant of charcoal rot of sorghum. J. Mycol. Pl. Path., 29:251-253 Deepak Kumar Srivastava and Heera Lal Yadav. 2008. Antifungal activity of some medicinal plants against Fusarium oxysporum f. sp. lycopersici. Ind. Phytopath., 61:99-102 Ganesan, T. 1993. Fungitoxic effect of wild plant leaf extracts. Geobios, 20:264-266 Karthekeyan, A. and Karunanidhi, K.1996. Influence of organic amendments on the intensity of Fusarium wilt of banana . Pl. Dis. Res., 11:180-181 Mishra, S.R. 2005. Plant Protection and Pest Management. Discovery Publishing House, Science, 304 p. Table 1. Effect of various plant extracts on mycelial growth, sclerotial formation and germination of Sclerotium rolfsii S.l No. Plant extract used Mycelial Per cent Inhibition (%) Sclerotial Inhibition growth inhibition of sclerotium germination (% over Control) (cm) of growth formation (%) after 72 h 1 Neem (Azadirachta indica) 1.73 80.61 11.00 5 95 2 Callistemon (Callistemon lanceolatus) 2.26 74.80 5.83 60 40 3 Periwinkle (Vinca rosea) 1.90 78.80 6.67 12 88 4 Ashoka (Polyalthia longifolia) 2.96 67.03 9.83 30 70 5 Curry leaf (Murraya koenigii) 5.90 34.40 3.16 70 30 6 Prosopis (Prosopis julifera) 4.26 52.59 4.50 50 50 7 Onion (Allium cepa) 5.83 35.18 3.20 55 45 8 Ginger (Zingiber officinale) 4.46 48.22 3.63 8 92 9 Check 8.96 0 99.00 100 0 SEM ± 0.117 0.404 2.041 CD (P= 0.05) 0.350 1.211 6.119 Effect of plant extracts on dry root rot of chilli J. Hortl. Sci. 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Antifungal characterstics of Vinca rosea extracts. Ind. Phytopath., 30:36-40 Raghavendra, M.P., Satish, S. and Raveesha, K.A. 2002. Prosopis juliflora Swartz: A potential plant for the management of fungal diseases of crops. In: Asian Cong. Mycol. Pl. Path., Ind. Soc. Mycol. Pl. Pathol., University of Mysore, p.136 Singh, R.K. and Dwivedi, R.S. 1989. Effect of plant parts and products on morphology and growth of Sclerotium rolfsiia foot root rot pathogen of barley. Acta Bot. Indica, 17:125-127 Seshakiran, K., Lingaraju, S. and Adiver, S.S. 2006. Effect of plant extracts on Sclerotium rolfsii, the incitant of stem rot of groundnut. J. Mycol. Pl. Path., 36:77-79 Sheoraj Singh, Prajapathi, R.K., Srivastava, S.S.L., Pandey, R.K. and Gupta, P.K.2007. Evaluation of different botanicals and non target pesticides against Sclerotium rolfsii causing collar rot of lentil. Ind. Phytopath., 60:499-501 Sonali and Gupta, A.K. 2004. Efficacy of plant materials on inhibition of sclerotial germination of Sclerotium rolfsii. J. Mycol. Pl. Path., 34:382-384 Sharma, S.K. and Gupta, V.K. 1995. Management of root rots of apple through soil amendments with plant materials. Pl. Dis. Res., 11:164-167 (MS Received 9 March 2010, Revised 3 June 2011) Bindu Madhavi et al J. Hortl. Sci. Vol. 6(2):156-158, 2011 Prinect Color Editor Page is color controlled with Prinect Color Editor 4.0.70 Copyright 2008 Heidelberger Druckmaschinen AG http://www.heidelberg.com You can view actual document colors and color spaces, with the free Color Editor (Viewer), a Plug-In from the Prinect PDF Toolbox. Please request a PDF Toolbox CD from your local Heidelberg office in order to install it on your computer. 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